Using Quality Systems that Produce Solid Data

About Us

Group of Clinical Research Associates

Our experienced staff has over 18 years of hands on clinical research knowledge and expertise in the Pharmaceutical and Biotechnology industry. We work with investigator sites as well as sponsor companies to reach the common trial goals of compliance, safety, and quality data collection through our monitoring, auditing, and training services.  Our knowledge base includes extensive experience in the following disease indications:

  • Oncology, Hematology, Respiratory, Gastroenterology, Diabetes , Cardiology, Central Nervous System disorders, Pain, Osteoporosis, and Alzheimer’s Disease.

Our clinical research consulting and training services are welcomed around the U.S. We assist pharmaceutical companies, biotech companies, government agencies, and clinical research sites located in Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Illinois, Indiana, Kansas, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Mexico, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, U.S. Virgin Islands, Utah, Vermont, Virginia, Washington, Washington, DC, West Virginia, Wisconsin, and Wyoming manage the safety and quality of their clinical trials.

Cities in which our staff have conducted trainings and monitoring include: Anchorage, AK; Atlanta, GA; Austin, TX; Chicago, IL; Colorado Springs, CO; Dallas, TX; Denver, Colorado; Indianapolis, IN; Las Vegas, NV; Los Angeles, CA; Miami, FL; Philadelphia, PA; San Antonio, TX; San Diego, CA; San Francisco, CA; San Jose, CA; Santa Clara, CA; Birmingham, AL; Jackson, MS; Houston, TX; Columbia, SC; Boston, MA; Memphis, TN; and Tampa, FL.